BEUDAMED
    39 results · 26ms · Sources: EU EUDAMED, US FDA

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    PIPET CURET

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Preat Implant Prosthetics

    FDA UDI
    Preat Corporation·00842092179314·Straumann® BL NC-compatible Scan Body Kit Conta...

    TruForm

    FDA UDI
    Rmo, Inc.·00885797099655·MAN 1ST MOLAR RT&LT 100 BANDS

    artVeneer life

    FDA UDI
    Merz Dental GmbH·D7092001545·artVeneer life upper anteriors, ITL, BL1

    Scanlan® VASCU-STATT® II approximator single-use bulldog clamp w/firmr pres

    FDA UDI
    SCANLAN INTERNATIONAL INC·00846159000603·Scanlan® VASCU-STATT® II approximator single-us...

    SENTRY EXPANDING INTRODUCER SHEATH (EIS)

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    SYSMEX AUTOMATED COAGULATION ANALYZER, MODEL CA-6000

    FDA 510(k)
    FDA Class 2 ·Hematology

    PTERYFIT IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·May 15, 2025

    PTERYFIT IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·May 15, 2025

    DRIVER SHAFT, T-15, SHORT

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code MDM·June 21, 2018

    DRIVER SHAFT, T-15, LONG

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

    DRIVER SHAFT, T-15, LONG

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

    DRIVER SHAFT, T-15, MEDIUM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

    DRIVER SHAFT, T-15, MEDIUM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

    DRIVER SHAFT, T-15, MEDIUM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

    3.0MM HEX DRIVER

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

    DRIVER SHAFT, T-15, MEDIUM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 14, 2021

    PTERYFIT IMPLANT

    FDA Adverse Event
    Injury ·NORIS MEDICAL LTD·Product code DZE·March 24, 2026

    ASR ACETABULAR IMPLANT 50

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·March 13, 2013

    RESTORE ULTRA

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code LGW·January 26, 2011